Cryopreservation of ovine primordial follicles using dimethyl sulfoxide

被引:18
作者
Amorim, CA [1 ]
Rodrigues, APR [1 ]
Rondina, D [1 ]
Gonçalves, PBD [1 ]
De Figueiredo, JR [1 ]
Giorgetti, A [1 ]
机构
[1] Univ Florence, Dipartimento Sci Zootecn, Lab Renzo Giuliani, Florence, Italy
关键词
primordial follicles; dimethyl sulfoxide; concentrations; toxicity test; cryopreservation; ovine; ovary;
D O I
10.1016/S0015-0282(02)04820-3
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To verify the viability of isolated primordial follicles after exposure to different concentrations of dimethyl sulfoxide (DMSO) and after cryopreservation. Design: Randomized control trial. Setting: Laboratorio Renzo Giuliani, University of Florence, Italy. Animal(s): Thirty- to 40-day-old lambs. Main Outcome Measure(s): Isolated primordial follicles were stained with trypan blue to evaluate the effect of different DMSO concentrations before and after the cryopreservation. Histological structure and follicular mortality were evaluated. Result(s): After the isolation procedure (control), a mean (+/-SE) of 800 +/- 23.86 live primordial follicles/mL were obtained. The number of live follicles in the toxicity test using the DMSO at 0, 0.5, 1.0, 1.5, 2.0, and 2.5 M was 782 +/- 193.96, 754 +/- 172.03, 778 +/- 191.58, 736 +/- 191.92, 476 +/- 122.9, and 316 +/- 83.52, respectively. The number of live follicles at 2.5 M was lower than that in the control procedure. After cryopreservation, the numbers decreased to 0 0 +/- 232 +/- 44.20, 636 +/- 161.82, 628 +/- 181.28, 208 +/- 11.57, and 184 +/- 47.07, respectively at 0, 0.5, 1.0, 1.5, 2.0, and 2.5 M. The number of live follicles at 0, 0.5, 2.0, and 2.5 M were lower than that in the control procedure. Conclusion(s): After cryopreservation, only DMSO concentrations of 1.0 and 1.5 M showed a number of live follicles similar to that of the control procedure. (Fertil Steril((R)) 2003;79(Suppl 1):682-6. 2003 by American Society for Reproductive Medicine.)
引用
收藏
页码:682 / 686
页数:5
相关论文
共 25 条
[11]   THE RECOVERY OF PREANTRAL FOLLICLES FROM OVARIES OF DOMESTIC CATS AND THEIR CHARACTERIZATION BEFORE AND AFTER CULTURE [J].
JEWGENOW, K ;
GORITZ, F .
ANIMAL REPRODUCTION SCIENCE, 1995, 39 (04) :285-297
[12]   Live offspring by in vitro fertilization of oocytes from cryopreserved primordial mouse follicles after sequential in vivo transplantation and in vitro maturation [J].
Liu, J ;
Van der Elst, J ;
Van den Broecke, R ;
Dhont, M .
BIOLOGY OF REPRODUCTION, 2001, 64 (01) :171-178
[13]  
Mazur P, 1977, Ciba Found Symp, P19
[14]  
Newton H, 1999, J REPROD FERTIL, V115, P141, DOI 10.1530/jrf.0.1150141
[15]  
Newton H, 1996, HUM REPROD, V11, P1487
[16]   Permeation of human ovarian tissue with cryoprotective agents in preparation for cryopreservation [J].
Newton, H ;
Fisher, J ;
Arnold, JRP ;
Pegg, DE ;
Faddy, MJ ;
Gosden, RG .
HUMAN REPRODUCTION, 1998, 13 (02) :376-380
[17]   The cryopreservation of ovarian tissue as a strategy for preserving the fertility of cancer patients [J].
Newton, H .
HUMAN REPRODUCTION UPDATE, 1998, 4 (03) :237-247
[18]  
Newton H, 1999, J REPROD FERTIL, V117, P27
[19]   Ovarian cryopreservation and transplantation: basic aspects [J].
Oktay, K ;
Karlikaya, GG ;
Aydin, BA .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2000, 169 (1-2) :105-108
[20]   REGENERATION OF RAT OVARIAN TISSUE GRAFTED AFTER EXPOSURE TO LOW TEMPERATURES [J].
PARKES, AS ;
SMITH, AU .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1953, 140 (901) :455-+